01 1Esteve Huayi Pharmaceutical Co. , Ltd.
02 1Glenmark Life Sciences Limited
03 1Organic Synthesis Chemicals Co., Ltd.
04 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
05 1Shiratori Pharmaceutical Co., Ltd.
06 1UBE Inc.
01 1Dedicated for manufacturing solifenacin succinate
02 4Solifenacin Succinate
03 1Solifenacin succinate production only
01 1China
02 1India
03 4Japan
Registration Number : 302MF10005
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2020-01-07
Latest Date of Registration : 2020-01-07
Registration Number : 301MF10071
Registrant's Address : Linhai Rd. , Yuecheng District Shaoxing, Zhejiang China
Initial Date of Registration : 2019-10-01
Latest Date of Registration : 2019-10-01
Registration Number : 306MF10112
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2024-08-22
Latest Date of Registration : 2024-08-22
Solifenacin succinate For manufacturing only
Registration Number : 301MF10110
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2019-12-20
Latest Date of Registration : 2019-12-20
Solifenacin succinate For manufacturing only
Registration Number : 301MF10095
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2019-11-19
Latest Date of Registration : 2019-11-19
Registration Number : 302MF10014
Registrant's Address : 3-10-4 Nihonbashi Ningyocho, Chuo-ku, Tokyo
Initial Date of Registration : 2020-01-27
Latest Date of Registration : 2022-09-29
A Solifenacin Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solifenacin Succinate, including repackagers and relabelers. The FDA regulates Solifenacin Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solifenacin Succinate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Solifenacin Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solifenacin Succinate supplier is an individual or a company that provides Solifenacin Succinate active pharmaceutical ingredient (API) or Solifenacin Succinate finished formulations upon request. The Solifenacin Succinate suppliers may include Solifenacin Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Solifenacin Succinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Solifenacin Succinate Drug Master File in Japan (Solifenacin Succinate JDMF) empowers Solifenacin Succinate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Solifenacin Succinate JDMF during the approval evaluation for pharmaceutical products. At the time of Solifenacin Succinate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Solifenacin Succinate suppliers with JDMF on PharmaCompass.
We have 6 companies offering Solifenacin Succinate
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